Preconditioning mesenchymal stromal cells with flagellin enhances the anti‑inflammatory ability of their secretome against lipopolysaccharide‑induced acute lung injury

Acute lung injury (ALI) is a complex condition frequently encountered in the clinical setting. The aim of the present study was to investigate the effect of conditioned media (CM) from human adipose‑derived mesenchymal stromal cells (MSCs) activated by flagellin (F‑CM), a Toll‑like receptor 5 ligand...

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Bibliographic Details
Main Authors: Li, Rui (Author) , Li, Yu (Author) , Dong, Xiaoyan (Author)
Format: Article (Journal)
Language:English
Published: July 28, 2020
In: Molecular medicine reports
Year: 2020, Volume: 22, Issue: 4, Pages: 2753-2766
ISSN:1791-3004
DOI:10.3892/mmr.2020.11380
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.3892/mmr.2020.11380
Verlag, kostenfrei, Volltext: https://www.spandidos-publications.com/10.3892/mmr.2020.11380
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Author Notes:Rui Li, Yu Li and Xiaoyan Dong
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Summary:Acute lung injury (ALI) is a complex condition frequently encountered in the clinical setting. The aim of the present study was to investigate the effect of conditioned media (CM) from human adipose‑derived mesenchymal stromal cells (MSCs) activated by flagellin (F‑CM), a Toll‑like receptor 5 ligand, on inflammation‑induced lung injury. In the in vitro study, RAW264.7 macrophages treated with F‑CM had a higher proportion of cells with the M2 phenotype, lower expression of pro‑inflammatory factors and stronger expression of anti‑inflammatory genes compared with the CM from normal adipose‑derived MSCs. Furthermore, in vivo experiments were performed in mice with ALI induced by intraperitoneal injection of lipopolysaccharide. F‑CM significantly alleviated the lung exudation, inhibited inflammatory cell recruitment in lung tissues and decreased the concentration of inflammatory factors in the bronchoalveolar lavage fluid. These findings indicated that F‑CM has superior anti‑inflammation ability compared with CM, and that it may represent a promising therapeutic approach to the treatment of inflammation‑induced ALI.
Item Description:Gesehen am 05.08.2025
Physical Description:Online Resource
ISSN:1791-3004
DOI:10.3892/mmr.2020.11380